FIGURE

Fig. 2

ID
ZDB-FIG-161110-9
Publication
Cheng et al., 2016 - Vinculin b deficiency causes epicardial hyperplasia and coronary vessel disorganization in zebrafish
Other Figures
All Figure Page
Back to All Figure Page
Fig. 2

The vclb gene is disrupted in the v12 mutant. (A) The zebrafish vclb gene is a homolog of human vinculin (VCL). (B) vclb mRNA expression as revealed by in situ hybridization is similar to EGFP expression patterns in the somites at 24 hpf and the heart at 48 hpf. Arrow points to the heart. (C) vclb is an alternative transcript corresponding to the vcla transcript variant without exon 19. No other alternative splicing transcripts are detected. odc (ornithine decarboxylase 1) is a loading control. RT–, without reverse transcriptase. (D) Diagram indicating that the transposon insertion in the v12 mutant causes fusion of EGFP with the N-terminal 261 amino acids of Vclb (NVclb). (E) NVclb-EGFP fusion protein expression detected with a GFP antibody in heterozygous and homozygous v12 mutant heart at 30 dpf. Size markers (kDa) are shown to the right. Gapdh provides a loading control. (F,G) Intact vclb, but not vcla, mRNA expression is blocked in the v12 mutant at 36 hpf as assayed by RT-PCR (F) and qRT-PCR (G). The expression level of vcla is the same among wild type, heterozygotes and v12 mutant. The qRT-PCR data are presented as mean±s.e.m. Two-tailed unpaired t-test; NS, not significant; ***P<0.001.

Expression Data
Genes:
Fish:
Anatomical Terms:
Stage Range: 75%-epiboly to Long-pec

Expression Detail
Antibody Labeling
Phenotype Data
Fish:
Observed In:
Stage: Prim-25

Phenotype Detail
Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Development